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The language of lizards: interpreting the function of visual displays of the Indian rock lizard, Psammophilus dorsalis (Agamidae)

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Abstract

The first step in understanding any communication system is to document signal diversity relative to the context of signalling (e.g. sex of the signaller and audience). Observation of 30 free-ranging rock lizards (Psammophilus dorsalis) on rock outcrops in southern India over a period of 18 months revealed that these lizards produce a complex array of ritualized signals involving push-ups (head-bobbing), dorsal flattening, extension of the legs or gular region, and tail-raising. Push-ups were performed by both sexes, usually after moving from one location to another. Push-ups were rarely accompanied by other postural modifications, and seem to function as non-directed signals. Dorsal flattening was elicited by birds flying overhead, and seems to make the lizard less conspicuous to predators. There was, nonetheless, a strong sex difference in the frequency of this behaviour, because the habitats used by males (open rocks) exposed them to more birds. Males displayed to females by extending their gular folds and arching their backs; other animals (e.g. squirrels, monkeys) also elicited the latter posture from both sexes. Leg extension was observed for both males and females, but in different contexts—males in response to conspecifics, females in response to other animals. Females raised their tails in response to encountering a male. Thus, these lizards have a complex repertoire of postures for predator evasion, for interaction with other species and with conspecifics, and for communicating sex-specific social information about gender (tail-raise) or dominance status (gular extension, leg extension).

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References

  • Andersson M (1982) Female choice selects for extreme tail length in a widowbird. Nature 299:818–820

    Article  Google Scholar 

  • Andersson M (1986) Evolution of condition-dependent sex ornaments and mating preferences: sexual selection based on viability differences. Evolution 40:804–816

    Google Scholar 

  • Baird TA, Timanus DK, Sloan CL (2003) Intra- and intersexual variation in social behavior: Effect of ontogeny, phenotype, resources and season. In: Fox SF, McCoy JK, Baird TA (eds) Lizard social behavior. The John Hopkins University Press, Baltimore, pp 7–46

    Google Scholar 

  • Baxter LR Jr (2003) Basal ganglia systems in ritualistic social displays: reptiles and humans; function and illness. Physiol Behav 79:451–460

    Article  PubMed  Google Scholar 

  • Blanco G, Puente JDL (2002) Multiple elements of the black-billed magpie’s tail correlate with variable honest information on quality in different age/sex classes. Anim Behav 63:217–225

    Article  Google Scholar 

  • Brattstrom BH (1971) Social and thermoregulatory behavior of the bearded dragon, Amphibolurus barbatus. Copeia 1971:484–497

    Google Scholar 

  • Brooks DR, Couldridge V (1999) Multiple sexual ornaments coevolve with multiple mating preferences. Am Nat 154:37–45

    Article  Google Scholar 

  • Bull CM (1988) Mate fidelity in an Australian lizard Trachydosaurus rugosus (Scincidae). Behav Ecol Sociobiol 23:45–49

    Article  Google Scholar 

  • Bull CM, Doherty M, Schultz LR, Pamula Y (1994) Recognition of offspring by females of the Australian skink, Tiliqua rugosa. J Herpetol 28:117–120

    Google Scholar 

  • Carpenter CC (1965) Aggression and social structure in iguanid lizards. In: Milstead WW (ed) Lizard ecology: a symposium. University of Missouri Press, Columbia, pp 87–105

    Google Scholar 

  • Carpenter CC, Ferguson GW (1977) Variation and evolution of stereotyped behavior in reptiles. In: Gans C, Tinkle DW (eds) Biology of reptilia: ecology and behavior, A, vol 7. Academic, New York, pp 335–554

    Google Scholar 

  • Carpenter CC, Badham JA, Kimble B (1970) Behavior patterns of three species of Amphibolurus (Agamidae). Copeia 1970:497–505

    Google Scholar 

  • Castellano S, Giacoma C, Dujsebayeva T (2000) Morphometric and advertisement call geographic variation in polyploid green toads. Biol J Linn Soc 70:341–360

    Article  Google Scholar 

  • Chappell MA, Zuk M, Kwan TH, Johnsen TS (1995) Energy cost of an avian vocal display: crowing in red jungle fowl. Anim Behav 49:255–257

    Article  Google Scholar 

  • Clutton-Brock TH, Guiness FE, Albon SD (1982) Red deer: behavior of two sexes. University of Chicago Press, Chicago

    Google Scholar 

  • Cooper WE, Greenberg N (1992) Reptilian coloration and behavior. In: Gans C, Crews D (eds) Biology of reptilia, physiology e hormones, brain and behavior, vol 18. University of Chicago Press, Chicago, pp 298–422

  • Davies NB (1992) Dunnock behavior and social evolution. Oxford University Press, Oxford

    Google Scholar 

  • DeCourcy KR, Jenssen TA (1994) Structure and use of male headbob signals by the lizard Anolis carolinensis. Anim Behav 47:251–262

    Article  Google Scholar 

  • Dugan B (1982) A field study of the headbob displays of male green iguanas (Iguana iguana): variation in form and context. Anim Behav 30:327–338

    Google Scholar 

  • Dyer FC (2002) The biology of the dance language. Annu Rev Entomol 47:917–949

    Article  PubMed  Google Scholar 

  • Evans MR (1991) The size of adornments of male scarlet-tufted malachite sunbirds varies with environmental conditions as predicted by handicap theories. Anim Behav 42:797–803

    Google Scholar 

  • Evans MR, Norris K (1996) The importance of carotenoids in signaling during aggressive interactions between male firemouth ciclids (Cichlasoma meeki). Behav Ecol 7:1–6

    Google Scholar 

  • Fitch HS (1987) Collecting and life history techniques. In: Siegel RA, Collins JT, Novak SS (eds) Snakes ecology and evolutionary biology. Macmillan, New York, pp 143–164

    Google Scholar 

  • Fox SF, McCoy JK, Baird TA (2003) The evolutionary study of social behavior and the role of lizards as model organisms. In: Fox SF, McCoy JK, Baird TA (eds) Lizard social behavior. John Hopkins University Press, Baltimore, pp xi-xiv

    Google Scholar 

  • Gibbons JRH (1979) The hind leg pushup displays of the Amphibolurus decresii species complex (Lacertilia: Agamidae). Copeia 1979:29–40

    Google Scholar 

  • Grant BW, Dunham AE (1988) Thermally imposed time constraints on the activity of the dessert lizard, Sceloporus merriami. Ecology 69:167–176

    Google Scholar 

  • Hasson O, Hibbard R, Ceballos G (1989) The pursuit deterrent function of tail-wagging in the zebra-tailed lizard (Callisaurus draconoides). Can J Zool 67:1205 –1209

    Google Scholar 

  • Heatwole H (1970) Thermal ecology of the desert dragon, Amphibolurus inermis. Ecol Monog 40:425–457

    Google Scholar 

  • Hews DK, Quinn VS (2003) Endocrinology of species differences in sexually dichromatic signals: Using organization and activation model in a phylogenetic frame work. In: Fox SF, McCoy JK, Baird TA (eds) Lizard social behavior. John Hopkins University Press, Baltimore, pp 253–277

    Google Scholar 

  • Holberton RL, Able KP, Wingfield JC (1989) Status signalling in dark-eyed juncos, Junco hyemalis: plumage manipulations and hormonal correlates of dominance. Anim Behav 37:681–689

    Article  Google Scholar 

  • Jenssen TA (1977) Evolution of anoline lizard display behavior. Am Zool 17:203–215

    Google Scholar 

  • Johnstone RA (1995) Honest advertisement of multiple qualities using multiple signals. J Theor Biol 177:87–94

    Article  Google Scholar 

  • Johnstone RA (1996) Multiple displays in animal communications: backup signals and multiple messages. Philos Trans Roy Soc Lond B 531:329–338

    Google Scholar 

  • Johnstone RA (1997) The evolution of animal signals. In: Krebs JR, Davies NB (eds) Behavioural ecology: an evolutionary approach, 4 edn. Blackwell Scientific, Oxford, pp 55–178

    Google Scholar 

  • Leal M (1999) Honest signalling during prey-predator interactions in the lizard Anolis cristatellus. Anim Behav 58:521–526

    Article  PubMed  Google Scholar 

  • Leal M, Rodriguez-Robles JA (1997) Signalling displays during predator-prey interactions in a Puerto Rican anole, Anolis cristatellus. Anim Behav 54:1147–1154

    Google Scholar 

  • Leal M, Fleishman LJ (2002) Evidence for habitat partitioning based on adaptation to environmental light in a pair of sympatric lizard species. Proc Roy Soc Lond B 269:351–359

    Article  Google Scholar 

  • Leger DW, Didrichson IA (1994) An assessment of data pooling and some alternatives. Anim Behav 48:823–832

    Article  Google Scholar 

  • Liebal K, Pika S, Tomasello M (2004) Social communication in siamangs (Symphalangus syndactylus): use of gestures and facial expression. Primates 45:41–57

    Article  PubMed  Google Scholar 

  • Macedonia JM, Clark DL (2001) Headbob display analysis of the Grand Cayman anole, Anolis conspersus. J Herpetol 35:300–310

    Google Scholar 

  • Marler P (2003) Variations among individuals: introduction. In: Fox SF, McCoy JK, Baird TA (eds) Lizard social behavior. The John Hopkins University Press, Baltimore, pp 3–6

    Google Scholar 

  • Martins EP (1991) Individual and sex differences in the use of the push-up display by the sagebrush lizard, Sceloporus graciosus. Anim Behav 41:403–416

    Google Scholar 

  • Martins EP (1993) Contextual use of the push-up display by the sagebrush lizard, Sceloporus graciosus. Anim Behav 45:25–36

    Article  Google Scholar 

  • Martins EP, Lamont J (1998) Estimating ancestral states of a communicative display: a comparative study of Cyclura rock iguanas. Anim Behav 55:1685–1706

    Article  PubMed  Google Scholar 

  • Martins EP, Labra A, Halloy M, Thompson JT (2004) Large-scale patterns of signal evolution: an interspecific study of Liolaemus lizard headbob displays. Anim Behav 68:453–463

    Article  Google Scholar 

  • McMann S (1993) Contextual signalling and the structure of dyadic encounters in Anolis carolinensis. Anim Behav 46:657–668

    Article  Google Scholar 

  • Melville J, Schulte II JA, Larson A (2001) A molecular phylogenetic study of ecological diversification in the Australian lizard genus Ctenophorus. J Exp Zool 291:339–353

    Article  PubMed  Google Scholar 

  • Møller AP, Pomiankowski A (1993) Why have birds got multiple sexual ornaments? Behav Ecol Sociobiol 32:167–176

    Google Scholar 

  • Mori A, Hikida T (1994) Field observations on the social behavior of the flying lizard, Draco Volans sumatranus, in Borneo. Copeia 1994:124–130

    Google Scholar 

  • Murphy JB, Lamoreaux WE, Carpenter CC (1978) Threatening behaviour in the angle-headed dragon, Goniocephalus dilophus (Reptilia, Lacertilia, Agamidae). J Herpetol 12:455–460

    Google Scholar 

  • O’Connor D, Shine R (2003) Lizards in “nuclear families”: a novel reptilian social system in Egernia saxatilis. Mole Ecol 12:743–752

    Article  Google Scholar 

  • Olsson M (1992) Contest success in relation to size and residency in male sand lizards, Lacerta agilis. Anim Behav 44:386–388

    Article  Google Scholar 

  • Olsson M (1994) Nuptial coloration in the sand lizard, Lacerta agilis: an intra-sexually selected cue to fighting ability. Anim Behav 48:607–613

    Article  Google Scholar 

  • Olsson M (1995) Forced copulation and costly female resistance behavior in the Lake Eyre dragon, Ctenophorus maculosus. Herpetologica 51:19–24

    Google Scholar 

  • Ord TJ, Blumstein DT (2002) Size constraints and the evolution of display complexity: why do large lizards have simple displays? Biol J Linn Soc 76:145–161

    Article  Google Scholar 

  • Ord TJ, Blumstein DT, Evans CS (2001) Intrasexual selection predicts the evolution of signal complexity in lizards. Proc Roy Soc Lond B 268:737–744

    Article  Google Scholar 

  • Podos J (2001) Correlated evolution of morphology and vocal signal structure in Darwin’s finches. Nature 409:185–188

    Article  PubMed  Google Scholar 

  • Prum RO (1998) Sexual selection and the evolution of mechanical sound production in manakins (Aves: Pipridae). Anim Behav 55:977–994

    Article  PubMed  Google Scholar 

  • Quinn VS, Hews DK (2000) Signals and behavioral responses are not coupled in males: aggression affected by replacement of an evolutionary lost color signal. Proc R Soc Lond B 267:755–758

    Article  Google Scholar 

  • Radder RS, Saidapur SK, Shanbhag BA (2005) Population density, microhabitat use and activity pattern of the Indian rock lizard, Psammophilus dorsalis (Agamidae). Curr Sci 89:560–565

    Google Scholar 

  • Radder RS, Saidapur SK, Shanbhag BA (2006) Big boys on the top: effects of body size, sex and reproductive state on perching behaviour in the tropical rock dragon, Psammophilus dorsalis. Anim Biol (in press)

    Google Scholar 

  • Sarkar HBD, Shivanandappa T (1989) Reproductive cycles of reptiles. In: Saidapur SK (ed) Reproductive cycles of Indian vertebrates. Allied Publishers Limited, New Delhi, pp 225–272

    Google Scholar 

  • Shanbhag BA (2002) Reproductive biology of Indian reptiles. Proc Indian Natl Sci Acad B 68:497–528

    Google Scholar 

  • Shine R (1990) Function and evolution of the frill of the frill neck lizard, Chlamydosaurus kingii (Sauria: Agamidae). Biol J Linn Soc 40:11–20

    Google Scholar 

  • Sinervo B, Lively CM (1996) The rock-paper-scissor game and the evolution of alternative male strategies. Nature 380:240–243

    Article  Google Scholar 

  • Sinervo B, Miles DB, Frankino WA, Klukowski M, DeNardo DF (2000) Testosterone, endurance, and Darwinian fitness: natural and sexual selection on the physiological bases of alternative male behaviors in side blotched lizards. Horm Behav 38:222–233

    Article  PubMed  Google Scholar 

  • Snowdon CT (1990) Language capacities of non-human animals. Yearbook of Phys Anthro 33:215–243

    Article  Google Scholar 

  • Stamps JA (1977) Social behavior and spacing patterns in lizards. In: Gans C, Tinkle DW (eds) Biology of reptilia: ecology and behavior, a, vol 7. Academic, New York, pp 335–354

  • Tokarz RR (1985) Body size as a factor determining dominance in staged agonistic encounters between male brown anoles (Anolis sagrei). Anim Behav 49:661–669

    Google Scholar 

  • Tomasello M, Zuberbuehler K (2002) Primate vocal and gestural communication. In: Bekoff M, Allen CS, Burghardt G (eds) The cognitive animal: empirical and theoretical perspectives on animal cognition. MIT Press, Cambridge, pp 293–329

    Google Scholar 

  • Watt MJ, Joss JMP (2003) Structure and function of visual displays produced by male Jacky dragon, Amphibolurus muricatus, during social interactions. Brain Behav Evol 61:172–183

    Article  PubMed  Google Scholar 

  • Whiting MJ, Nagy KA, Bateman PW (2003) Evolution and maintenance of social status-signaling badges: experimental manipulations in lizards. In: Fox SF, McCoy JK, Baird TA (eds) Lizard social behavior. The John Hopkins University Press, Baltimore, pp 7–46

    Google Scholar 

  • Wiens JJ (1999) Phylogenetic evidence for multiple losses of a sexually selected character in phrynosomatid lizards. Proc Roy Soc Lond B 266:1529–1535

    Article  Google Scholar 

  • Yabuta S (2002) Uncertainty in partner recognition and the tail-up display in monogamous butterfly fish. Anim Behav 63:165–173

    Article  Google Scholar 

Download references

Acknowledgements

This work was supported by a Council of Scientific and Industrial Research’s (CSIR, India) Associateship awarded to RSR, Special Assistance Programme (SAP-II) University Grant Commission (UGC, India) sanctioned to Department of Zoology Karnatak University Dharwad and by the Australian Research Council (to RS). Authors thank Professor R.Gadagkar, Center for Ecological Sciences, Indian Institute of Science, Bangalore for his keen interest in this study. We thank Principal Chief Conservator of Forests, Bangalore for permitting us to study rock lizards.

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Correspondence to Bhagyashri A. Shanbhag.

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Radder, R.S., Saidapur, S.K., Shine, R. et al. The language of lizards: interpreting the function of visual displays of the Indian rock lizard, Psammophilus dorsalis (Agamidae). J Ethol 24, 275–283 (2006). https://doi.org/10.1007/s10164-006-0192-8

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